[go: up one dir, main page]

FI964218A7 - Compounds with blood pressure-lowering, cardioprotective, anti-anemia and fat-dissolving properties - Google Patents

Compounds with blood pressure-lowering, cardioprotective, anti-anemia and fat-dissolving properties Download PDF

Info

Publication number
FI964218A7
FI964218A7 FI964218A FI964218A FI964218A7 FI 964218 A7 FI964218 A7 FI 964218A7 FI 964218 A FI964218 A FI 964218A FI 964218 A FI964218 A FI 964218A FI 964218 A7 FI964218 A7 FI 964218A7
Authority
FI
Finland
Prior art keywords
compounds
cardioprotective
anemia
fat
lowering
Prior art date
Application number
FI964218A
Other languages
Finnish (fi)
Swedish (sv)
Other versions
FI964218L (en
FI964218A0 (en
Inventor
Cynthia A Fink
Alfred P Spada
Michael R Myers
Original Assignee
Aventis Pharma Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aventis Pharma Inc filed Critical Aventis Pharma Inc
Publication of FI964218A0 publication Critical patent/FI964218A0/en
Publication of FI964218A7 publication Critical patent/FI964218A7/en
Publication of FI964218L publication Critical patent/FI964218L/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32—Nitrogen atom
    • C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/052—Imidazole radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16—Purine radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Saccharide Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Föreliggande uppfinning avser adenosinderivat och analoger, som är aktiva som adenosinagonister och som är användbara som antihypertensiva, hjärtskyddande, anti-ischemiska och antilipolytiska läkemedel, farmaceutiska kompositioner, som inkluderar dessa föreningar, och användning av dem vid behandling av hypertoni, myokardischemi, minskande av ischemisk skada och storleken av en myokardinfarkt orsakad av myokardischemi, och behandling av hyperli-pidemi och hyperkolesterolemi, och förfaranden och mellanprodukter för framställning av dessa föreningar.The present invention relates to adenosine derivatives and analogues which are active as adenosine agonists and which are useful as antihypertensive, cardioprotective, anti-ischemic and antilipolytic drugs, pharmaceutical compositions which include these compounds, and their use in the treatment of hypertension, myocardial ischemia, reducing ischemic damage and the size of a myocardial infarction caused by myocardial ischemia, and treating hyperlipidemia and hypercholesterolemia, and processes and intermediates for the preparation of these compounds.

FI964218A 1994-04-19 1995-04-19 Compounds with blood pressure-lowering, cardioprotective, anti-anemia and fat-dissolving properties FI964218L (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22988294A 1994-04-19 1994-04-19
US08/316,761 US5561134A (en) 1990-09-25 1994-10-03 Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
PCT/US1995/004800 WO1995028160A1 (en) 1994-04-19 1995-04-19 Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties

Publications (3)

Publication Number Publication Date
FI964218A0 FI964218A0 (en) 1996-10-18
FI964218A7 true FI964218A7 (en) 1996-12-17
FI964218L FI964218L (en) 1996-12-17

Family

ID=26923699

Family Applications (1)

Application Number Title Priority Date Filing Date
FI964218A FI964218L (en) 1994-04-19 1995-04-19 Compounds with blood pressure-lowering, cardioprotective, anti-anemia and fat-dissolving properties

Country Status (28)

Country Link
US (2) US5561134A (en)
EP (2) EP1006115A3 (en)
JP (1) JPH09512020A (en)
KR (1) KR970702045A (en)
CN (1) CN1086704C (en)
AP (1) AP699A (en)
AT (1) ATE260106T1 (en)
AU (1) AU684635B2 (en)
BG (1) BG63799B1 (en)
BR (1) BR9507327A (en)
CA (1) CA2188147C (en)
CZ (1) CZ289528B6 (en)
DE (1) DE69532608T2 (en)
DK (1) DK0758897T3 (en)
EE (1) EE9600156A (en)
ES (1) ES2217279T3 (en)
FI (1) FI964218L (en)
HU (1) HUT75331A (en)
NO (1) NO317727B1 (en)
NZ (1) NZ284357A (en)
OA (1) OA10464A (en)
PL (1) PL182942B1 (en)
PT (1) PT758897E (en)
RO (1) RO119225B1 (en)
RU (1) RU2166319C2 (en)
SI (1) SI9520055A (en)
SK (1) SK284039B6 (en)
WO (1) WO1995028160A1 (en)

Families Citing this family (83)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5721263A (en) * 1993-06-07 1998-02-24 Takeda Chemical Industries, Ltd. Pharmaceutical composition for angiotensin II-mediated diseases
US5792776A (en) * 1994-06-27 1998-08-11 Cytomed, Inc., Compounds and methods for the treatment of cardiovascular, inflammatory and immune disorders
AU711057B2 (en) * 1995-05-30 1999-10-07 Aventis Pharma S.A. 2-azabicyclo(2,2,1)heptane derivatives, their preparation and their application
US6992188B1 (en) 1995-12-08 2006-01-31 Pfizer, Inc. Substituted heterocyclic derivatives
US6376472B1 (en) 1996-07-08 2002-04-23 Aventis Pharmaceuticals, Inc. Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
UA51716C2 (en) * 1996-07-08 2002-12-16 Авентіс Фармасьютікалз Продактс Інк. combinations possessing hypotensive, cardioprotective, anti-ishemic, and antilipolytic agents, a pharmaceutical composition and METHOD OF TREATMENT
US5747474A (en) * 1996-07-29 1998-05-05 Immune Modulation, Inc. Immunosuppression by administration of N6,N6 -disubstituted cAMP's, analogues thereof, and related nucleosides
WO1998016539A1 (en) * 1996-10-14 1998-04-23 Novo Nordisk A/S Novel therapeutically active adenosine derivatives
GB9723590D0 (en) * 1997-11-08 1998-01-07 Glaxo Group Ltd Chemical compounds
GB9723566D0 (en) * 1997-11-08 1998-01-07 Glaxo Group Ltd Chemical compounds
PT1175420E (en) * 1998-12-21 2003-08-29 Aventis Pharma Inc PROCESS FOR THE PREPARATION OF N6-SUBSTITUTED DERIVATIVES OF DESAZA-ADENOSINE
KR20010089751A (en) 1998-12-31 2001-10-08 오흘러 로스 제이. Process for preparing N6-substituted deaza-adenosine derivatives
US7378400B2 (en) * 1999-02-01 2008-05-27 University Of Virginia Patent Foundation Method to reduce an inflammatory response from arthritis
US7018365B2 (en) 1999-05-21 2006-03-28 Micro Therapeutics, Inc. Threaded syringe with quick stop
US6576619B2 (en) * 1999-05-24 2003-06-10 Cv Therapeutics, Inc. Orally active A1 adenosine receptor agonists
DE19951701A1 (en) * 1999-10-27 2001-05-03 Aventis Pharma Gmbh Use of 2-imidazolyl-substituted carbinols for the manufacture of a medicament for the treatment or prophylaxis of diseases caused by ischemic conditions
US6368573B1 (en) * 1999-11-15 2002-04-09 King Pharmaceuticals Research And Development, Inc. Diagnostic uses of 2-substituted adenosine carboxamides
US20020045613A1 (en) * 2000-04-27 2002-04-18 Heinz Pauls 1-aroyl-piperidinyl benzamidines
GB0013407D0 (en) * 2000-06-02 2000-07-26 Astrazeneca Ab Forms of a chemical compound
US6670334B2 (en) 2001-01-05 2003-12-30 University Of Virginia Patent Foundation Method and compositions for treating the inflammatory response
NZ532062A (en) * 2001-10-01 2006-09-29 Univ Virginia 2-propynyl adenosine analogues having A2 adenosine recepter agonist activity and compositions thereof to treat inflammatory responses
US7414036B2 (en) 2002-01-25 2008-08-19 Muscagen Limited Compounds useful as A3 adenosine receptor agonists
US7086397B2 (en) * 2002-02-16 2006-08-08 Graham Lindley Spruiell Patient usable emergency medical kit
CN101392012A (en) * 2002-02-19 2009-03-25 Cv医药有限公司 Partial and full agonists of A1 adenosine receptors
CA2480471A1 (en) * 2002-03-26 2003-10-02 Forbes Medi-Tech Inc. A process for the extraction of anthocyanins from black rice and composition thereof
DE60318192T2 (en) * 2002-04-10 2008-04-30 The University Of Virginia Patent Foundation USE OF A2A ADENOSINE RECEPTOR AGONISTS AND ANTI-PATHOGENIC AGENTS CONTAINING COMBINATIONS IN THE TREATMENT OF INFLAMMATORY DISEASES
US7265111B2 (en) * 2002-06-27 2007-09-04 Sanofi-Aventis Deutschland Gmbh Adenosine analogues and their use as pharmaceutical agents
MXPA06005894A (en) * 2003-12-19 2006-06-27 Hoffmann La Roche Comt inhibitors.
EP1574508A1 (en) 2004-01-30 2005-09-14 Lonza AG Process for the preparation of acetals and ketals of 3-amimo-5-(hydroxymethyl)-cyclopentane-1,2-diols and their derivatives and salts
EP1732905A1 (en) * 2004-03-31 2006-12-20 Lexicon Genetics Incorporated 2-aminomethylthiazole-5-carboxamides as protein kinase modulators
US7576069B2 (en) * 2004-08-02 2009-08-18 University Of Virginia Patent Foundation 2-polycyclic propynyl adenosine analogs having A2A agonist activity
WO2006023272A1 (en) * 2004-08-02 2006-03-02 University Of Virginia Patent Foundation 2-polycyclic propynyl adenosine analogs having a2a agonist activity
EP2266994B1 (en) * 2004-08-02 2013-04-03 University Of Virginia Patent Foundation 2-propynyl adenosine analgos with modified 5'-ribose groups having A2A agonist activity
GT200500281A (en) * 2004-10-22 2006-04-24 Novartis Ag ORGANIC COMPOUNDS.
EP1831225A2 (en) 2004-11-19 2007-09-12 The Regents of the University of California Anti-inflammatory pyrazolopyrimidines
NZ565461A (en) * 2005-08-30 2011-08-26 Abbott Lab Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV)
WO2007092936A2 (en) * 2006-02-08 2007-08-16 University Of Virginia Patent Foundation Method to treat gastric lesions
WO2007120972A2 (en) 2006-02-10 2007-10-25 University Of Virginia Patent Foundation Method to treat sickle cell disease
US7649098B2 (en) * 2006-02-24 2010-01-19 Lexicon Pharmaceuticals, Inc. Imidazole-based compounds, compositions comprising them and methods of their use
US20080032960A1 (en) 2006-04-04 2008-02-07 Regents Of The University Of California PI3 kinase antagonists
US8188063B2 (en) * 2006-06-19 2012-05-29 University Of Virginia Patent Foundation Use of adenosine A2A modulators to treat spinal cord injury
TW200920355A (en) * 2007-09-06 2009-05-16 Lexicon Pharmaceuticals Inc Compositions and methods for treating immunological and inflammatory diseases and disorders
WO2009046448A1 (en) 2007-10-04 2009-04-09 Intellikine, Inc. Chemical entities and therapeutic uses thereof
US8058259B2 (en) * 2007-12-20 2011-11-15 University Of Virginia Patent Foundation Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9H-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as A2AR agonists
US8193182B2 (en) 2008-01-04 2012-06-05 Intellikine, Inc. Substituted isoquinolin-1(2H)-ones, and methods of use thereof
MX2010007419A (en) 2008-01-04 2010-11-12 Intellikine Inc Certain chemical entities, compositions and methods.
WO2009114874A2 (en) 2008-03-14 2009-09-17 Intellikine, Inc. Benzothiazole kinase inhibitors and methods of use
US8637542B2 (en) 2008-03-14 2014-01-28 Intellikine, Inc. Kinase inhibitors and methods of use
RU2363453C1 (en) * 2008-03-25 2009-08-10 Олег Николаевич Моисеев Method of treating trichomoniasis in cattle
US20110224223A1 (en) * 2008-07-08 2011-09-15 The Regents Of The University Of California, A California Corporation MTOR Modulators and Uses Thereof
JP5788316B2 (en) 2008-07-08 2015-09-30 インテリカイン， エルエルシー Kinase inhibitors and methods of use
JP5731978B2 (en) 2008-09-26 2015-06-10 インテリカイン， エルエルシー Heterocyclic kinase inhibitor
AU2009305669A1 (en) 2008-10-16 2010-04-22 The Regents Of The University Of California Fused ring heteroaryl kinase inhibitors
US8476282B2 (en) 2008-11-03 2013-07-02 Intellikine Llc Benzoxazole kinase inhibitors and methods of use
AR075899A1 (en) * 2009-03-20 2011-05-04 Onyx Therapeutics Inc PROTEASA INHIBITING CRYSTALLINE EPOXYCETON TRIPEPTIDES
CA2760791C (en) 2009-05-07 2017-06-20 Intellikine, Inc. Heterocyclic compounds and uses thereof
WO2011047384A2 (en) 2009-10-16 2011-04-21 The Regents Of The University Of California Methods of inhibiting ire1
CA2789950C (en) 2010-02-18 2018-09-04 High Point Pharmaceuticals, Llc Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof
US8759535B2 (en) 2010-02-18 2014-06-24 High Point Pharmaceuticals, Llc Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof
CA2799579A1 (en) 2010-05-21 2011-11-24 Intellikine, Inc. Chemical compounds, compositions and methods for kinase modulation
JP2013545749A (en) 2010-11-10 2013-12-26 インフィニティー ファーマシューティカルズ， インコーポレイテッド Heterocyclic compounds and uses thereof
AR084824A1 (en) 2011-01-10 2013-06-26 Intellikine Inc PROCESSES TO PREPARE ISOQUINOLINONES AND SOLID FORMS OF ISOQUINOLINONAS
EP2678018A4 (en) 2011-02-23 2015-09-30 Intellikine Llc Combination of kanase inhibitors and uses thereof
CA2842190A1 (en) 2011-07-19 2013-01-24 Infinity Pharmaceuticals Inc. Heterocyclic compounds and uses thereof
HK1198443A1 (en) 2011-07-19 2015-04-24 无限药品股份有限公司 Heterocyclic compounds and uses thereof
CA2846431A1 (en) 2011-08-29 2013-03-07 Infinity Pharmaceuticals Inc. Heterocyclic compounds and uses thereof
EP2751112B1 (en) 2011-09-02 2019-10-09 The Regents of The University of California Substituted pyrazolo[3,4-d]pyrimidines and uses thereof
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
US8828998B2 (en) 2012-06-25 2014-09-09 Infinity Pharmaceuticals, Inc. Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
EP2900673A4 (en) 2012-09-26 2016-10-19 Univ California MODULATION OF IRE1
MX375194B (en) 2012-11-01 2025-03-06 Infinity Pharmaceuticals Inc TREATMENT OF CANCER USING PI3 KINASE ISOFORM MODULATORS.
US9481667B2 (en) 2013-03-15 2016-11-01 Infinity Pharmaceuticals, Inc. Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
MY175778A (en) 2013-10-04 2020-07-08 Infinity Pharmaceuticals Inc Heterocyclic compounds and uses thereof
WO2015051241A1 (en) 2013-10-04 2015-04-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CN106414456B (en) * 2013-10-23 2018-12-14 中央研究院 Compounds for the prevention and treatment of neurodegenerative diseases and pain
PT3119397T (en) 2014-03-19 2022-04-11 Infinity Pharmaceuticals Inc Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders
US20150320755A1 (en) 2014-04-16 2015-11-12 Infinity Pharmaceuticals, Inc. Combination therapies
WO2016054491A1 (en) 2014-10-03 2016-04-07 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
WO2016089648A1 (en) 2014-12-01 2016-06-09 Vtv Therapeutics Llc Bach 1 inhibitors in combination with nrf2 activators and pharmaceutical compositions thereof
CN114230571B (en) 2015-09-14 2025-07-08 无限药品股份有限公司 Solid forms of isoquinolinones, methods of making, compositions comprising, and methods of using the same
WO2017161116A1 (en) 2016-03-17 2017-09-21 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
WO2017214269A1 (en) 2016-06-08 2017-12-14 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
KR20190033526A (en) 2016-06-24 2019-03-29 인피니티 파마슈티칼스, 인코포레이티드 Combination therapy

Family Cites Families (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL128629C (en) * 1966-05-07
DE2524284A1 (en) * 1966-12-21 1976-10-28 Boehringer Mannheim Gmbh Cardiovascular-active nitrogen substd. adenosine derivs. - prepd. by reacting amines with 6-(halo or mercapto)-9-purinyl ribosides
BE768925A (en) * 1970-06-30 1971-11-03 Takeda Chemical Industries Ltd ADENOSINE DERIVATIVES AND METHOD OF PREPARATION
DE2059922A1 (en) * 1970-12-05 1972-06-15 Boehringer Mannheim Gmbh Novel N (6) aralkyl-adenosine derivatives and processes for making the same
DE2205002A1 (en) * 1972-02-03 1973-08-09 Merck Patent Gmbh N (6)-bicycloalkyl-adoensines - with activity on blood circulation and oxygenation
DE2136624A1 (en) * 1971-07-22 1973-02-08 Boehringer Mannheim Gmbh N (6) -SUBSTITUTED ADENOSINE DERIVATIVES AND METHOD FOR PREPARING THE SAME
DE2139107A1 (en) * 1971-08-04 1973-02-15 Merck Patent Gmbh N(6)-subst adenosine derivs - with coronary circulatory etc activity
DE2151013C2 (en) * 1971-10-08 1983-04-28 Schering Ag, 1000 Berlin Und 4619 Bergkamen Process for the preparation of 6-amino- and 2,6-diaminopurine nucleosides which are optionally substituted in the N → 6 → position
US3864483A (en) * 1972-03-22 1975-02-04 Abbott Lab Adenosine-5{40 -carboxylic acid amides
US3931401A (en) * 1972-10-21 1976-01-06 Abbott Laboratories 1,N6 -etheno-5'-adenosine carboxamides for increasing coronary sinus partial pressure of oxygen
US3914415A (en) * 1973-06-14 1975-10-21 Abbott Lab Adenosine-5{40 -carboxylic acid amides
US4167565A (en) * 1976-11-08 1979-09-11 Abbott Laboratories Adenosine-5'-carboxamides and method of use
NO154918C (en) * 1977-08-27 1987-01-14 Bayer Ag ANALOGUE PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVE DERIVATIVES OF 3,4,5-TRIHYDROXYPIPERIDINE.
US4340730A (en) * 1980-06-09 1982-07-20 G. D. Searle & Co. N6 -Substituted adenosines
JPS59219284A (en) * 1983-05-27 1984-12-10 Toyo Jozo Co Ltd 3'-deoxyneplanocin a and its preparation
CA1239397A (en) * 1983-08-01 1988-07-19 James A. Bristol N.sup.6-substituted adenosines
US4501735A (en) * 1983-12-05 1985-02-26 Warner-Lambert Company N6-(1- and 2-benzocycloalkyl) adenosines
EP0300145A3 (en) * 1984-04-18 1989-08-30 Whitby Research Incorporated N-6 phenyl substituted adenosine derivatives as cardiac vasodilators
US4657897A (en) * 1984-06-22 1987-04-14 Warner-Lambert Company N6 -substituted adenosines for treating pain
US4657898A (en) * 1984-06-22 1987-04-14 Warner-Lambert Company N6 -substituted adenosines and method of use
US5310731A (en) * 1984-06-28 1994-05-10 Whitby Research, Inc. N-6 substituted-5'-(N-substitutedcarboxamido)adenosines as cardiac vasodilators and antihypertensive agents
US4582823A (en) * 1984-08-15 1986-04-15 Warner-Lambert Company Method for treating schizophrenia and medicaments therefor
US4663313A (en) * 1984-10-26 1987-05-05 Warner-Lambert Company N6 -tricyclic adenosines for treating hypertension
US4683223A (en) * 1985-09-09 1987-07-28 Warner-Lambert Company N6 -Benzopyrano-and benzothiopyrano adenosines and methods of use
US4593019A (en) * 1984-10-26 1986-06-03 Warner-Lambert Company N6 -tricyclic adenosines
AU575438B2 (en) * 1984-10-26 1988-07-28 Warner-Lambert Company N6 - substituted deoxyribose analogues of adenosines
US4636493A (en) * 1985-01-25 1987-01-13 Warner-Lambert Company Benzothien-3-yl adenosine; benzothien-3-yl adenosine, S-oxide; and benzothien-3-yl, S,S-dioxide adenosine compounds
US4600707A (en) * 1985-01-25 1986-07-15 Warner-Lambert Company Benzothien-3-yl adenosine; benzothien-3-yl adenosine, S-oxide; and benzothien-3-yl, S,S-dioxide adenosine compounds
DE3529497A1 (en) * 1985-08-17 1987-02-26 Boehringer Mannheim Gmbh N (ARROW HIGH) 6 (ARROW HIGH) -DISUBSTITUTED PURINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS
US4738954A (en) * 1985-11-06 1988-04-19 Warner-Lambert Company Novel N6 -substituted-5'-oxidized adenosine analogs
US4755594A (en) * 1986-01-31 1988-07-05 Warner-Lambert Company N6 -substituted adenosines
AU8276187A (en) * 1986-10-31 1988-05-25 Warner-Lambert Company Selected n6-substituted adenosines having selective a2 binding activity
WO1988003148A2 (en) * 1986-10-31 1988-05-05 Warner-Lambert Company Heteroaromatic derivatives of adenoside
US5063233A (en) * 1986-11-14 1991-11-05 Ciba-Geigy Corporation N9 -cyclopentyl-substituted adenine derivatives useful as adenosine receptor agonists
US4954504A (en) * 1986-11-14 1990-09-04 Ciba-Geigy Corporation N9 -cyclopentyl-substituted adenine derivatives having adenosine-2 receptor stimulating activity
IL84414A0 (en) * 1986-11-14 1988-04-29 Ciba Geigy Ag N9-cyclopentyl-substituted adenine derivatives
JPH0723394B2 (en) * 1986-11-27 1995-03-15 日本臓器製薬株式会社 Novel adenosine derivative and pharmaceutical composition containing the compound as an active ingredient
HU198950B (en) * 1986-12-15 1989-12-28 Sandoz Ag Process for producing new furanuronic acid derivatives and pharmaceutical compositions comprising such compounds
US4968697A (en) * 1987-02-04 1990-11-06 Ciba-Geigy Corporation 2-substituted adenosine 5'-carboxamides as antihypertensive agents
PT86660B (en) * 1987-02-04 1992-02-28 Ciba Geigy Ag PROCESS FOR THE PREPARATION OF ADENOSIN-5'-CARBOXAMIDE DERIVATIVES
CA1340361C (en) * 1987-04-24 1999-02-02 Whitby Research, Inc. N6-substituted 9-methyladenines: a new class of adenosine receptor antagonists
GB8729994D0 (en) * 1987-12-23 1988-02-03 Glaxo Group Ltd Chemical compounds
AU3820989A (en) * 1988-08-02 1990-02-08 Ciba-Geigy Ag 7-amino-3-beta-d-ribofuranosyl-3h-imidazo(4,5-b) pyridin-5-amine derivatives
US4977144A (en) * 1988-08-02 1990-12-11 Ciba-Geigy Corporation Imidazo[4,5-b]pyridine derivatives as cardiovascular agents
GB2226027B (en) * 1988-12-13 1992-05-20 Sandoz Ltd Adenosine derivatives,their production and use
JPH0725785B2 (en) * 1989-01-11 1995-03-22 日本臓器製薬株式会社 Adenosine derivative and pharmaceutical composition containing the compound as an active ingredient
GB8916480D0 (en) * 1989-07-19 1989-09-06 Glaxo Group Ltd Chemical process
ES2095960T3 (en) * 1990-09-25 1997-03-01 Rhone Poulenc Rorer Int COMPOUNDS THAT HAVE ANTI-HYPERTENSIVE AND ANTI-ISCHEMICAL PROPERTIES.
HUT61567A (en) * 1990-12-07 1993-01-28 Sandoz Ag Process for producing new pharmaceutical compositions comprising 2'-o-alkyladenosine derivatives and for producing 6-cyclohexyl-2'-o-methyladenosinehydrate

Also Published As

Publication number Publication date
US5561134A (en) 1996-10-01
AP9600904A0 (en) 1997-01-31
BG100963A (en) 1997-08-29
BR9507327A (en) 1997-10-07
ATE260106T1 (en) 2004-03-15
ES2217279T3 (en) 2004-11-01
EP1006115A2 (en) 2000-06-07
SI9520055A (en) 1997-06-30
EP1006115A3 (en) 2000-06-28
CN1148811A (en) 1997-04-30
HUT75331A (en) 1997-05-28
EE9600156A (en) 1997-06-16
NO964438L (en) 1996-10-18
RO119225B1 (en) 2004-06-30
PL182942B1 (en) 2002-05-31
BG63799B1 (en) 2003-01-31
PT758897E (en) 2004-07-30
HU9602829D0 (en) 1996-12-30
AP699A (en) 1998-12-01
DE69532608D1 (en) 2004-04-01
AU2294995A (en) 1995-11-10
PL316961A1 (en) 1997-02-17
SK134096A3 (en) 1997-05-07
NZ284357A (en) 2001-06-29
WO1995028160A1 (en) 1995-10-26
KR970702045A (en) 1997-05-13
DE69532608T2 (en) 2005-01-05
CA2188147A1 (en) 1995-10-26
NO317727B1 (en) 2004-12-13
FI964218L (en) 1996-12-17
FI964218A0 (en) 1996-10-18
CZ289528B6 (en) 2002-02-13
EP0758897A4 (en) 1997-11-19
CA2188147C (en) 2001-04-03
EP0758897B1 (en) 2004-02-25
RU2166319C2 (en) 2001-05-10
MX9604999A (en) 1998-05-31
HK1011294A1 (en) 1999-07-09
CZ303296A3 (en) 1997-05-14
CN1086704C (en) 2002-06-26
DK0758897T3 (en) 2004-05-03
AU684635B2 (en) 1997-12-18
SK284039B6 (en) 2004-08-03
NO964438D0 (en) 1996-10-18
OA10464A (en) 2002-04-03
EP0758897A1 (en) 1997-02-26
US5736554A (en) 1998-04-07
JPH09512020A (en) 1997-12-02

Similar Documents

Publication Publication Date Title
FI964218A7 (en) Compounds with blood pressure-lowering, cardioprotective, anti-anemia and fat-dissolving properties
CA2259538A1 (en) Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
EP0550631A4 (en) Compounds having antihypertensive and anti-ischemic properties
BG100635A (en) SUBSTITUTED N- (INDOL-2-CARBONYL) -BETA-ALANINAMIDES AND THEIR PRODUCTS AS ANTI-DIABETIC MEDICINAL PRODUCTS
ES2178037T3 (en) CYCLOSPORINE DERIVATIVES, ITS PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM.
BR0009292A (en) Use of pyridoxine compounds to treat cardiovascular pathologies and related pathologies
PT951474E (en) NEW DERIVATIVES OF CICLOSPORIN ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM
AP2002002458A0 (en) Compounds for the treatment of ischemia.
DK1140993T3 (en) Glycopeptide derivatives and pharmaceutical preparations containing them
BR0200782A (en) Compounds for the treatment of ischemia
RU94031126A (en) CYCLIC UREA AND THEIR ANALOGUES SUITABLE AS RETROVIRUS PROTEASE INHIBITORS, METHOD FOR TREATING VIRAL INFECTIONS, PHARMACEUTICAL COMPOSITION
AR002751A1 (en) TETRAHYDROFURAN ANTIFUNGALS, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND THE USE OF THE COMPOUNDS TO PREPARE USEFUL PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF FUNGAL INFECTIONS
BR0311535A (en) Use of substituted cyanopyrrolidines and combination preparations containing them for the treatment of hyperlipidemia and associated diseases
ES2052732T3 (en) 2 ', 3'-DIDESOXI-3'-FLUOROTIMIDINE AND RELATED COMPOUNDS FOR THE TREATMENT OF ADENOVIRUS INFECTIONS.
NO20014347L (en) Synergistic inhibition of viral replication by long chain hydrocarbons and nucleoside analogues
ES2019840A6 (en) PROCEDURE TO PREPARE NEW DERIVATIVES OF TIENO-TRIAZOLO-DIAZEPINA.
NO983444L (en) Benzo (c) quinolizine derivatives, their preparation and use as 5 <alfa> reductase inhibitors
DK0904272T3 (en) Dihydrobenzofuran and related compounds useful as anti-inflammatory agents
WO1999052936A3 (en) Arginine peptide analogs useful as fibroblast growth factor antagonists
ES2025164B3 (en) CIS- AND TRANS-STYLBENE AND ITS COMPOSITION FOR THE TREATMENT OF HYPERTENSION.

Legal Events

Date Code Title Description
PC Transfer of assignment of patent

Owner name: AVENTIS PHARMACEUTICALS INC.